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Midodrine HCl - 21695-181-00 - (Midodrine Hydrochloride)

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Drug Information of Midodrine HCl

Product NDC: 21695-181
Proprietary Name: Midodrine HCl
Non Proprietary Name: Midodrine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Midodrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Midodrine HCl

Product NDC: 21695-181
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076514
Marketing Category: ANDA
Start Marketing Date: 20020702

Package Information of Midodrine HCl

Package NDC: 21695-181-00
Package Description: 100 TABLET in 1 BOTTLE (21695-181-00)

NDC Information of Midodrine HCl

NDC Code 21695-181-00
Proprietary Name Midodrine HCl
Package Description 100 TABLET in 1 BOTTLE (21695-181-00)
Product NDC 21695-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midodrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020702
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name MIDODRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Midodrine HCl


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